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RDX

1000 μg/mL in acetonitrile, ampule of 1.2 mL, certified reference material, Cerilliant®

Synonym(e):

Hexahydro-1,3,5-trinitro-1,3,5-triazine, Hexahydro-1,3,5-trinitro-1,3,5-triazine solution

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About This Item

Empirische Formel (Hill-System):
C3H6N6O6
CAS-Nummer:
121-82-4
Molekulargewicht:
222.12
MDL-Nummer:
MFCD00458725
UNSPSC-Code:
41116107
NACRES:
NA.24

Qualität

certified reference material

Leistungsmerkmale

Snap-N-Spike®/Snap-N-Shoot®

Verpackung

ampule of 1.2 mL

Hersteller/Markenname

Cerilliant®

Konzentration

1000 μg/mL in acetonitrile

Anwendung(en)

environmental

Format

single component solution

Lagertemp.

−20°C

SMILES String

O=[N+]([O-])N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1

InChI

1S/C3H6N6O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H2

InChIKey

XTFIVUDBNACUBN-UHFFFAOYSA-N

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Rechtliche Hinweise

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

Piktogramme

FlameExclamation mark
GHS02,GHS07

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

35.6 °F - closed cup

Flammpunkt (°C)

2 °C - closed cup

Analysenzertifikate (COA)

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Hao-Ping Chen et al.
Applied and environmental microbiology, 78(21), 7798-7800 (2012-08-28)
Whole-genome sequencing, transcriptomic analyses, and metabolic reconstruction were used to investigate Gordonia sp. strain KTR9's ability to catabolize a range of compounds, including explosives and steroids. Aspects of this mycolic acid-containing actinobacterium's catabolic potential were experimentally verified and compared with
Anat Bernstein et al.
Environmental science & technology, 47(1), 479-484 (2012-12-12)
The explosive Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) is known to be degraded aerobically by various isolates of the Rhodococcus species, with denitration being the key step, mediated by Cytochrome P450. Our study aimed at gaining insight into the RDX degradation mechanism by Rhodococcus
Karl K Irikura
The journal of physical chemistry. A, 117(10), 2233-2241 (2013-02-05)
The explosive nitramine RDX (1,3,5-trinitrohexahydro-s-triazine) is thought to decompose largely by homolytic N-N bond cleavage, among other possible initiation reactions. Density-functional theory (DFT) calculations indicate that the resulting secondary aminyl (R2N·) radical can abstract an oxygen atom from NO2 or
Thomas J Bruno et al.
Journal of chromatography. A, 1286, 192-199 (2013-03-13)
In previous work, dynamic headspace vapor collection on short, porous layer open tubular (PLOT) capillary columns maintained at low temperature was introduced. In this paper, that metrology is extended with the introduction of a small in situ pyrolysis platform that
Muhammad Imran Khan et al.
Journal of microbiology and biotechnology, 22(10), 1311-1323 (2012-10-19)
In the present work, current knowledge on the potential fate, microbial degradation, and toxicity of hexahydro- 1,3,5-trinitro-1,3,5-triazine (RDX) was thoroughly reviewed, focusing on the toxicological assessment of a variety of potential RDX degradation pathways in bacteria and fungi. The present
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